Bert Ba de Vries
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders 6
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 3
- Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research 2
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- Congenital heart defects research 2
- RNA modifications and cancer 1
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- Family and Disability Support Research 1
- Co-authors
- Martinus F. NiermeijerBen A. OostraD. J. J. HalleyEveline Wesby–van SwaayJ. O. Van HemelJ. P. FrynsMerlin G. ButlerDavid A. Koolen
- Journals
- Epilepsia (1 paper)Journal of Medical Genetics (3 papers)Europe PMC (PubMed Central) (2 papers)
- Partner nations
- NetherlandsAustraliaCanada
In The Last Decade
Bert Ba de Vries
6 papers receiving 293 citations
Peers
Comparison fields: 5 of 44
- Genetics 270
- Cognitive Neuroscience 121
- Molecular Biology 169
- Developmental Neuroscience 8
- Cellular and Molecular Neuroscience 18
Countries citing papers authored by Bert Ba de Vries
This map shows the geographic impact of Bert Ba de Vries's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Bert Ba de Vries with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bert Ba de Vries more than expected).
Fields of papers citing papers by Bert Ba de Vries
This network shows the impact of papers produced by Bert Ba de Vries. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Bert Ba de Vries. The network helps show where Bert Ba de Vries may publish in the future.
Co-authorship network
The 20 scholars most cited alongside Bert Ba de Vries, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 20 | |
| 2 | WAC-Related Intellectual Disability | 2017 | 1 |
| 3 | 15q13.3 Microdeletion | 2015 | 0 |
| 4 | KANSL1-Related Intellectual Disability Syndrome | 2013 | 6 |
| 5 | 1998 | 190 | |
| 6 | 1997 | 15 | |
| 7 | 1993 | 73 |
About Bert Ba de Vries
Bert Ba de Vries is a scholar working on Genetics, Cognitive Neuroscience and Clinical Psychology, having authored 7 papers that have together received 305 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers), Autism Spectrum Disorder Research (2 papers), Congenital heart defects research (2 papers), Family and Disability Support Research (1 paper) and RNA modifications and cancer (1 paper). The work is most often cited by research in Genetics (270 citations), Cognitive Neuroscience (121 citations) and Molecular Biology (169 citations). Bert Ba de Vries has collaborated with scholars based in Netherlands, Australia and Canada. Frequent co-authors include Martinus F. Niermeijer, Ben A. Oostra, D. J. J. Halley, Eveline Wesby–van Swaay, J. O. Van Hemel, J. P. Fryns, Merlin G. Butler, David A. Koolen, Simone Mandelstam and Kenneth A. Myers. Their work appears in journals such as Epilepsia, Journal of Medical Genetics and Europe PMC (PubMed Central).
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.